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癌症诊断与治疗中表观遗传调控的分子基础。

Molecular basis of epigenetic regulation in cancer diagnosis and treatment.

作者信息

Tulsyan Sonam, Aftab Mehreen, Sisodiya Sandeep, Khan Asiya, Chikara Atul, Tanwar Pranay, Hussain Showket

机构信息

Division of Cellular and Molecular Diagnostics (Molecular Biology Group), ICMR- National Institute of Cancer Prevention and Research, Noida, India.

Symbiosis School of Biological Sciences, Symbiosis International (Deemed University), Pune, India.

出版信息

Front Genet. 2022 Aug 24;13:885635. doi: 10.3389/fgene.2022.885635. eCollection 2022.

Abstract

The global cancer cases and mortality rates are increasing and demand efficient biomarkers for accurate screening, detection, diagnosis, and prognosis. Recent studies have demonstrated that variations in epigenetic mechanisms like aberrant promoter methylation, altered histone modification and mutations in ATP-dependent chromatin remodelling complexes play an important role in the development of carcinogenic events. However, the influence of other epigenetic alterations in various cancers was confirmed with evolving research and the emergence of high throughput technologies. Therefore, alterations in epigenetic marks may have clinical utility as potential biomarkers for early cancer detection and diagnosis. In this review, an outline of the key epigenetic mechanism(s), and their deregulation in cancer etiology have been discussed to decipher the future prospects in cancer therapeutics including precision medicine. Also, this review attempts to highlight the gaps in epigenetic drug development with emphasis on integrative analysis of epigenetic biomarkers to establish minimally non-invasive biomarkers with clinical applications.

摘要

全球癌症病例数和死亡率不断上升,需要高效的生物标志物用于准确的筛查、检测、诊断和预后评估。最近的研究表明,异常启动子甲基化、组蛋白修饰改变以及ATP依赖的染色质重塑复合物突变等表观遗传机制的变化在致癌事件的发生发展中起重要作用。然而,随着研究的不断深入和高通量技术的出现,其他表观遗传改变在各种癌症中的影响也得到了证实。因此,表观遗传标记的改变可能具有临床应用价值,作为早期癌症检测和诊断的潜在生物标志物。在本综述中,讨论了关键表观遗传机制及其在癌症病因中的失调,以解读癌症治疗(包括精准医学)的未来前景。此外,本综述试图突出表观遗传药物开发中的差距,重点是对表观遗传生物标志物进行综合分析,以建立具有临床应用价值的微创生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021a/9449878/41dc2b2d7798/fgene-13-885635-g001.jpg

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